Zimmer Segmental System — Class II medical device recall Z-1219-2015
Terminated recall by Zimmer, Inc., reported 2015-03-11, distributed in TX. PMMA coating does not meet specifications. Area of the stem may be missing PMMA coating.
| Recall number | Z-1219-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2015-02-05 |
| Classified | 2015-02-27 |
| Reported by FDA | 2015-03-11 |
| Terminated | 2015-09-23 |
| Distributed | TX |
| Quantity | 1 units |
| Lot numbers | 62866438 |
| Model numbers | 00-5852-052-10 |
Product
Zimmer Segmental System (ZSS) Cemented Stem / ZSS Cemented Stem, Smooth Stem Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non-Porous, Uncemented.
Reason for recall
PMMA coating does not meet specifications. Area of the stem may be missing PMMA coating.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1219-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.